FDA applicant
Happersberger Otopront GmbH
FDA records 1 decision for Happersberger Otopront GmbH (Germany, GR) in 1993: 1 510(k) clearance. All are in product code ETF (Unit, Examining/Treatment, Ent). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Happersberger Otopront GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Happersberger Otopront GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
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